Efficacy and safety of semaglutide for weight management: evidence from the STEP program.
Postgrad Med · 2022
Last updated 2026-05-28The STEP program tested semaglutide, a GLP-1 drug, for weight management in adults with overweight or obesity. Across five trials, a once-weekly 2.4 mg dose led to significant and sustained weight loss compared to placebo, along with improvements in heart and metabolism-related risk factors. Side effects were mostly mild to moderate stomach issues that went away over time. The drug was generally well tolerated.
AI summary of the abstract below.
| Journal | Postgrad Med, 2022 |
|---|---|
| Citations | 39 |
| Relative citation ratio | 3.41 |
| NIH percentile | 87 |
| Molecules | semaglutide |
| Conditions studied | Obesity |
Abstract
Obesity is a global health challenge. It is a multifactorial, complex, and progressive disease associated with various health complications and increased mortality. Lifestyle modifications are central to weight management but may be insufficient to maintain clinically meaningful weight loss. Pharmacotherapies are recommended as an adjunct to lifestyle interventions to induce and sustain clinically meaningful weight loss and reduce the risk of comorbidities in appropriate patients. Glucagon-like peptide-1 is an incretin metabolic hormone responsible for a range of physiological effects, including glucose and appetite regulation. Several glucagon-like peptide-1 receptor agonists (GLP-1RAs) have been approved for the treatment of type 2 diabetes since 2005 including exenatide (short- and extended-release), lixisenatide, liraglutide, dulaglutide, albiglutide, and semaglutide. Of these, semaglutide (subcutaneous) and liraglutide are currently US Food and Drug Administration (FDA)-approved for chronic weight management in patients with or without diabetes. The phase 3 Semaglutide Treatment Effect in People with obesity (STEP) program was designed to investigate the effect of semaglutide versus placebo on weight loss, safety, and tolerability in adults with overweight or obesity. Following the submission of the results of the STEP 1-4 trials, the FDA approved once-weekly subcutaneous semaglutide 2.4 mg for chronic weight management in people with overweight or obesity in April 2021. Data from the program demonstrated that semaglutide (2.4 mg once weekly) achieved significant and sustained weight loss, together with improvements in cardiometabolic risk factors compared with placebo, and was generally well tolerated, with a safety profile consistent with other GLP-1RAs. The most common adverse events reported in STEP 1-5 were gastrointestinal events, which were transient, mild-to-moderate in severity, and typically resolved without permanent treatment discontinuation. This article reviews the data from STEP 1-5 and highlights clinically relevant findings for primary care providers.
Verbatim abstract via PubMed 36691309 ↗
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